Percussionaire — Class I medical device recall Z-3208-2024
Ongoing recall by Percussionaire Corporation, reported 2024-10-09, distributed nationwide. Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary per
| Recall number | Z-3208-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Percussionaire Corporation, Sandpoint, ID, United States |
| Recall initiated | 2024-08-21 |
| Classified | 2024-09-27 |
| Reported by FDA | 2024-10-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CH, IL, JP, RU, TR |
| Quantity | 2,523 units |
| Reason classes | labeling |
| Lot numbers | 230612, 240326, 240418, 240610, 240620, WO03688, WO03748, WO03846, WO04061, WO04356, WO04398, WO04553, WO04596, WO04625, WO04656, WO04714, WO04756, WO04827, WO04884, WO05019, WO06020, WO07010, WO07066 |
| Model numbers | P5-TEE-20 |
Product
Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve
Reason for recall
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3208-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.